| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:77418676-77418880 | Rare:45 | ||||
| chr5:77851781-77851913 | Common:2; Rare:31 | ||||
| chr5:77936156-77936303 | Common:1; Rare:19 | ||||
| chr5:78359895-78360036 | Common:1; Rare:43 | ||||
| chr5:78361417-78361512 | Rare:17 | ||||
| chr5:78547647-78547822 | Rare:37 | ||||
| chr5:78568349-78568529 | Common:1; Rare:32 | ||||
| chr5:78568779-78568809 | Rare:2 | ||||
| chr5:78908476-78908628 | Common:3; Rare:32 | ||||
| chr5:78984539-78985049 | Common:10; Rare:187; Clinvar:9; Clinvar (benign):1; Clinvar (pathogenic):5 | ||||
| chr5:79134088-79134158 | Rare:14 | ||||
| chr5:79237312-79237360 | Rare:15 | ||||
| chr5:79416626-79416776 | Rare:29 | ||||
| chr5:79513384-79513447 | Rare:14 | ||||
| chr5:79517776-79517893 | Rare:20 |